5 research outputs found

    Stereoselective Synthesis of (+)- α

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    PEG-400 as an efficient and recyclable reaction medium for the synthesis of 2-aryl-2-methyl-4,5-diphenyl-2,3- dihydro-2<i>H</i>-imidazoles

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    <p>A productive natural method has been produced for the synthesis of 2-aryl-2-methyl-4,5-diphenyl-2,3-dihydro-2<i>H</i>-imidazoles in great yields under catalyst free-conditions utilizing polyethylene glycol (PEG-400) as a green reaction medium. The highlights of this new method are shorter reaction times, good yields, room temperature, and use of nontoxic, inexpensive, and recyclable PEG-400.</p

    Convenient and Scalable Synthesis of 2,3-Dihydroquinazolin-4(1<i>H</i>)-one Derivatives and Their Anticancer Activities

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    <div><p></p><p>An efficient and mild InBr<sub>3</sub>-catalyzed approach to synthesize 2,3-dihydroquinazolin-4(1<i>H</i>)-one derivatives (<b>3a–3aa</b>) has been developed. Notably, all the products were isolated by recrystallization and the reaction is accessible on a gram scale. Moreover, the reactions only require 10–60 min. All the synthesized compounds were evaluated for their in vitro anticancer activity against four human cancer cell lines.</p></div
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